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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429481Generated: October 30, 2026

Potassium Carbonate → ethyl 2-(3-(1-methyl-1H-pyrazol-5-yl)phenyl)acetate

https://huagongshe.com/reaction/1429481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-DioxaneHCID 31275—
Reactant5-Bromo-1-methyl-1H-pyrazoleHCID 17933381—
ReactantEthyl 2-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetateHCID 53217140—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventWaterHCID 962—
Productethyl 2-(3-(1-methyl-1H-pyrazol-5-yl)phenyl)acetateHCID 9024156370.4%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of ethyl 2-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetate (500 mg, 1.72 mmol), 5-bromo-1-methyl-1H-pyrazole (252 mg, 1.57 mmol), K2CO3 (651 mg, 4.71 mmol) and Pd(dppf)Cl2 (20 mg) in a solution of dioxane (10 mL) and H2O (2.5 mL) was stirred at 120° C. for 30 min under microwave. The catalyst was filtered through a pad of celite and the filtrate concentrated. The residue was purified by column chromatography to give the desired product (270 mg, Yield 70%) and used directly in the next step. LCMS (m/z): 245.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940726B2
Source datasetuspto-grants-2015_01
ORD IDord-3cb252d8132443479f4cfffe8eb85d4d
Source noteuspto-grants-2015_01